| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128149212-128149586 | Rare:89 | ||||
| chr9:128160008-128160403 | Common:2; Rare:93 | ||||
| chr9:128191468-128191657 | Rare:58 | ||||
| chr9:128191750-128191853 | Common:1; Rare:25 | ||||
| chr9:128275900-128276307 | Common:5; Rare:177 | ||||
| chr9:128322406-128322636 | Common:1; Rare:65 | ||||
| chr9:128322729-128322928 | Common:3; Rare:93; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128340440-128340753 | Common:2; Rare:97 | ||||
| chr9:128371159-128371425 | Common:1; Rare:101 | ||||
| chr9:128504628-128504782 | Rare:67; Clinvar:5 | ||||
| chr9:128552398-128552607 | Rare:77; Clinvar:1 | ||||
| chr9:128630042-128630342 | Common:4; Rare:76; Clinvar (benign):3 | ||||
| chr9:128635740-128635846 | Rare:30 | ||||
| chr9:128683361-128683446 | Common:1; Rare:11 | ||||
| chr9:128683502-128683804 | Rare:57 |